HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → Methyl 4-bromo-2-(p-chlorophenyl)-5-(trifluoromethyl)pyrrole-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Methyl 2-(p-chlorophenyl)-5-(trifluoromethyl)pyrrole-3-carboxylate | HCID 11034029 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Sodium Sulfite | HCID 24437 | — |
| Product | Methyl 4-bromo-2-(p-chlorophenyl)-5-(trifluoromethyl)pyrrole-3-carboxylate | HCID 20093623 | 82.4% |
Reaction Steps
Bromine (2.3 mL, 43.7 mmol) is added to a solution of methyl 2-(p-chlorophenyl)-5-(trifluoromethyl)pyrrole-3-carboxylate (8.44 g, 29.2 mmol) and sodium acetate (3.6 g, 43.7 mmol) in acetic acid. The reaction mixture is stirred for 30 minutes, diluted with a 0.4 wt/wt% sodium sulfite solution and extracted with diethyl ether. The organic extracts are combined, washed with saturated sodium hydrogen carbonate solution, dried over anhydrous Na2SO4 and concentrated in vacuo to obtain an oil which solidifies to give the title product as a solid (9.2 g) which is identified by 1H and 13C NMR spectral analyses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05389669 |
| Source dataset | uspto-grants-1995_02 |
| ORD ID | ord-cbcceaab31b44c629c1fc89c07cd980f |
| Source note | uspto-grants-1995_02 |